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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500121Generated: October 25, 2026

6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine → 6-((2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl)methyl)quinoline

https://huagongshe.com/reaction/500121

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amineHCID 57516523—
Reactant2-Chloro-3-(quinolin-6-yl)propanalHCID 57516537—
SolventIsopropanolHCID 3776—
Product6-((2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl)methyl)quinolineHCID 57971188—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (800 mg, 2.97 mmol) and 2-chloro-3-quinolin-6-ylpropanal (784 mg, 3.57 mmol) in isopropyl alcohol (10.0 mL) in a sealed tube was heated at 110° C. for 48 h. After the reaction mixture was cooled to ambient temperature, the product was precipitated and collected by filtration. The mother liquor was concentrated and the residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate, water, brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified on a silica gel column with methanol in dichloromethane (0-6%) to give the desired product. (65%) LCMS: (M+H)=434.0/436.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-a8fcf12b5a9945f4bc7fd8996d67fe46
Source noteuspto-grants-2010_08